Canonical Allele Identifier: CA481334073

Gene: PAH

Linked Data

• MyVariant Identifiers: chr12:g.103310900A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102917122A>C , CM000674.2:g.102917122A>C	GRCh38
NC_000012.11:g.103310900A>C , CM000674.1:g.103310900A>C	GRCh37
NC_000012.10:g.101835030A>C	NCBI36
NG_008690.1:g.5481T>G
NG_008690.2:g.46289T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553106.6:c.9T>G MANE Select	ENSP00000448059.1:p.Thr3=
ENST00000307000.7:c.-139T>G	ENSP00000303500.2:n.-139T>G
ENST00000546844.1:c.9T>G	ENSP00000446658.1:p.Thr3=
ENST00000547319.1:n.320T>G
ENST00000549111.5:n.105T>G
ENST00000551337.5:c.9T>G	ENSP00000447620.1:p.Thr3=
ENST00000551988.5:n.98T>G
ENST00000553106.5:c.9T>G	ENSP00000448059.1:p.Thr3=
ENST00000635500.1:n.29-4224T>G
NM_000277.1:c.9T>G	NP_000268.1:p.Thr3=
XM_011538422.1:c.9T>G	XP_011536724.1:p.Thr3=
NM_000277.2:c.9T>G	NP_000268.1:p.Thr3=
NM_001354304.1:c.9T>G	NP_001341233.1:p.Thr3=
XM_017019370.2:c.9T>G	XP_016874859.1:p.Thr3=
NM_000277.3:c.9T>G MANE Select	NP_000268.1:p.Thr3=
NM_001354304.2:c.9T>G	NP_001341233.1:p.Thr3=